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Pulmonary Vein Isolation vs Sham Intervention in Symptomatic Atrial Fibrillation: The SHAM-PVI Randomized Clinical Trial.
Dulai, Rajdip; Sulke, Neil; Freemantle, Nick; Lambiase, Pier D; Farwell, David; Srinivasan, Neil T; Tan, Stuart; Patel, Nikhil; Graham, Adam; Veasey, Rick A.
Afiliação
  • Dulai R; Cardiology Research Department, Eastbourne District General Hospital, East Sussex Hospitals NHS Trust, Eastbourne, United Kingdom.
  • Sulke N; Institute of Cardiovascular Science, University College London, London, United Kingdom.
  • Freemantle N; Mid and South Essex NHS Foundation Trust, Essex Cardiothoracic Centre, Basildon, United Kingdom.
  • Lambiase PD; Retired.
  • Farwell D; Institute for Clinical Trials and Methodology, University College London, London, United Kingdom.
  • Srinivasan NT; Institute of Cardiovascular Science, University College London, London, United Kingdom.
  • Tan S; Mid and South Essex NHS Foundation Trust, Essex Cardiothoracic Centre, Basildon, United Kingdom.
  • Patel N; Mid and South Essex NHS Foundation Trust, Essex Cardiothoracic Centre, Basildon, United Kingdom.
  • Graham A; Circulatory Health Research Group, Medical Technology Research Centre, School of Medicine, Anglia Ruskin University, Chelmsford, United Kingdom.
  • Veasey RA; Mid and South Essex NHS Foundation Trust, Essex Cardiothoracic Centre, Basildon, United Kingdom.
JAMA ; 2024 Sep 02.
Article em En | MEDLINE | ID: mdl-39221629
ABSTRACT
Importance There are concerns that pulmonary vein isolation for atrial fibrillation may have a profound placebo effect, but no double-blind randomized clinical trials have been conducted.

Objective:

To determine whether pulmonary vein isolation is more effective than a sham procedure for improving outcomes in atrial fibrillation. Design, Setting, and

Participants:

Double-blind randomized clinical trial conducted at 2 tertiary centers in the UK between January 2020 and March 2024 among patients with symptomatic paroxysmal or persistent atrial fibrillation. Major exclusion criteria included long-standing persistent atrial fibrillation, prior left atrium ablation, other arrhythmias requiring ablative therapy, a left atrium of 5.5 cm or larger, and ejection fraction of less than 35%. Intervention Participants were randomly assigned to receive pulmonary vein isolation with cryoablation (n = 64) or a sham procedure with phrenic nerve pacing (n = 62). Main Outcomes and

Measures:

The primary end point was atrial fibrillation burden at 6 months, excluding a 3-month blanking period. Secondary outcomes included quality-of-life measures, time to events, and safety. Atrial fibrillation burden was measured by an implantable loop recorder.

Results:

A total of 126 participants were randomized (mean age, 66.8 years; 89 men [70.63%]; 20.63% with paroxysmal atrial fibrillation). The absolute mean atrial fibrillation burden change from baseline to 6 months was 60.31% in the ablation group and 35.0% in the sham group (geometric mean difference, 0.25; 95% CI, 0.15-0.42; P < .001). The estimated difference in the overall Atrial Fibrillation Effect on Quality of Life score at 6 months, favoring catheter ablation, was 18.39 points (95% CI, 11.48-25.30 points). The Short Form 36 general health score also improved substantially more with ablation, with an estimated difference of 9.27 points at 6 months (95% CI, 3.78-14.76 points). Conclusions and Relevance Pulmonary vein isolation resulted in a statistically significant and clinically important decrease in atrial fibrillation burden at 6 months, with substantial improvements in symptoms and quality of life, compared with a sham procedure. Trial Registration ClinicalTrials.gov Identifier NCT04272762.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article